> Markdown version of [/jobs/ext/4082960-test-engineer](https://www.wearedevelopers.com/jobs/ext/4082960-test-engineer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Test Engineer - **Company:** Stryker - **Location:** Belfast, UK - **Salary:** £33,300.0 - £55,600.0 - **Contract:** Temporary contract - **Skills:** Iq/oq/pq, Performance Monitor - **Published:** October 24, 2026 - **Apply:** https://dejobs.org/x/x/2680EC8EF00442C0AE5BEC398BE014DE/job/ ## About the Role * Level 6 Degree in Biomedical/Electronic Engineering or equivalent technical experience is required. * Knowledge of Quality systems and requirements of regulated environments * Knowledge of the medical devices industry and associated regulation * Knowledge of lean manufacturing principles and practices * Demonstrable analytical & problem-solving skills, a process improvement orientation, and the ability to handle multiple tasks in a fast-paced and results-oriented environment. * Strong communication and influencing skills with both internal and external agents. * Fostering a working environment of continuous improvement * Excellent presentation and written / verbal communication skills. * Capable of working autonomously * A team player, with a flexible approach. * Capable of training manufacturing team members ## Description * Provide design, technical and operational support to test processes to meet business goals and objectives. * Support manufacturing process design, validation and implementation for Pad-Pak capacity expanding. * Provide Technical support for Test equipment and process onsite and offsite and ensure compliance with calibration schedule and requirements. * Support all capital acquisition activity from specifying equipment, contract negotiation, Installation, and validation. * Develop or review of test process documents including user requirements, functional specifications, risk assessment, design description, and traceability matrices. * Development and implementation of appropriate supporting documentation, SOPs, and process work instructions compliant with current Good Manufacturing Practices (GMP) * Line performance monitoring, and the compilation and execution of structured event plans to remediate systemic issues that drive sub-optimal performance. * Develop, implement, or review process validation plans, protocols, and reports associated with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). * Assist in the evaluation of out-of-specification results and associated corrective actions. * Actively interfacing with cross-functional team members and 3rd party Vendors, and always practicing good teamwork in support of the day-to-day operating requirements, and in pursuit of achieving the business targets * Delivers and presents technical and/or training presentations to management, employees, and contractors. * Observing the Quality Management Systems requirements on site at all times * Adherence to, and enforcement of all Environment Health and Safety (EHS) requirements on site * All other duties as assigned.